The potential for bacteria from carbon-limited deep terrestrial environments to participate in chlorine cycling.


Journal

FEMS microbiology ecology
ISSN: 1574-6941
Titre abrégé: FEMS Microbiol Ecol
Pays: England
ID NLM: 8901229

Informations de publication

Date de publication:
23 05 2022
Historique:
received: 15 12 2021
revised: 07 04 2022
accepted: 29 04 2022
pubmed: 6 5 2022
medline: 26 5 2022
entrez: 5 5 2022
Statut: ppublish

Résumé

Bacteria capable of dehalogenation via reductive or hydrolytic pathways are ubiquitous. Little is known, however, about the prevalence of bacterial dechlorination in deep terrestrial environments with a limited carbon supply. In this study we analyzed published genomes from three deep terrestrial subsurface sites: a deep aquifer in Western Siberia, the Sanford Underground Research Facility in South Dakota, USA, and the Soudan Underground Iron Mine (SUIM) in Minnesota, USA to determine if there was evidence to suggest that microbial dehalogenation was possible in these environments. Diverse dehalogenase genes were present in all analyzed metagenomes, with reductive dehalogenase and haloalkane dehalogenase genes the most common. Taxonomic analysis of both hydrolytic and reductive dehalogenase genes was performed to explore their affiliation; this analysis indicated that at the SUIM site, hydrolytic dehalogenase genes were taxonomically affiliated with Marinobacter species. Because of this affiliation, experiments were also performed with Marinobacter subterrani strain JG233 ('JG233'), an organism containing three predicted hydrolytic dehalogenase genes and isolated from the SUIM site, to determine whether hydrolytic dehalogenation was an active process and involved in growth on a chlorocarboxylic acid. Presence of these genes in genome appears to be functional, as JG233 was capable of chloroacetate dechlorination with simultaneous chloride release. Stable isotope experiments combined with confocal Raman microspectroscopy demonstrated that JG233 incorporated carbon from 13C-chloroacetate into its biomass. These experiments suggest that organisms present in these extreme and often low-carbon environments are capable of reductive and hydrolytic dechlorination and, based on laboratory experiments, may use this capability as a competitive advantage by utilizing chlorinated organic compounds for growth, either directly or after dechlorination.

Identifiants

pubmed: 35511595
pii: 6577122
doi: 10.1093/femsec/fiac054
pii:
doi:

Substances chimiques

Chlorides 0
Chloroacetates 0
Halogens 0
Chlorine 4R7X1O2820
Carbon 7440-44-0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of FEMS.

Auteurs

Susma Bhattarai (S)

Department of Civil, Environmental and Geo- Engineering, University of Minnesota Twin Cities, Minneapolis, MN 55455, United States.

Hanna Temme (H)

AECOM, 800 LaSalle Ave, Minneapolis, MN 55402, United States.

Abhiney Jain (A)

BioTechnology Institute, University of Minnesota Twin Cities, Saint Paul, MN 55108, United States.

Jonathan P Badalamenti (JP)

University of Minnesota Genomics Center, University of Minnesota Twin Cities, Minneapolis, MN 55455, United States.

Jeffrey A Gralnick (JA)

BioTechnology Institute, University of Minnesota Twin Cities, Saint Paul, MN 55108, United States.
Plant and Microbial Biology, University of Minnesota Twin Cities, Saint Paul, MN 55108, United States.

Paige J Novak (PJ)

Department of Civil, Environmental and Geo- Engineering, University of Minnesota Twin Cities, Minneapolis, MN 55455, United States.
BioTechnology Institute, University of Minnesota Twin Cities, Saint Paul, MN 55108, United States.

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Classifications MeSH